CN102471275B - Smac模拟物 - Google Patents

Smac模拟物 Download PDF

Info

Publication number
CN102471275B
CN102471275B CN201080031798.6A CN201080031798A CN102471275B CN 102471275 B CN102471275 B CN 102471275B CN 201080031798 A CN201080031798 A CN 201080031798A CN 102471275 B CN102471275 B CN 102471275B
Authority
CN
China
Prior art keywords
cancer
carcinoma
compound
cell
pharmaceutical composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201080031798.6A
Other languages
English (en)
Chinese (zh)
Other versions
CN102471275A (zh
Inventor
S.M.康顿
邓一军
M.G.拉波特
S.R.里平
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Medville Co., Ltd.
Original Assignee
TetraLogic Pharmaceuticals Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43411387&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CN102471275(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by TetraLogic Pharmaceuticals Corp filed Critical TetraLogic Pharmaceuticals Corp
Publication of CN102471275A publication Critical patent/CN102471275A/zh
Application granted granted Critical
Publication of CN102471275B publication Critical patent/CN102471275B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/05Dipeptides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/555Heterocyclic compounds containing heavy metals, e.g. hemin, hematin, melarsoprol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/03Peptides having up to 20 amino acids in an undefined or only partially defined sequence; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/07Tetrapeptides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/06Radiation therapy using light
    • A61N5/0613Apparatus adapted for a specific treatment
    • A61N5/062Photodynamic therapy, i.e. excitation of an agent
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/10X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/02Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06008Dipeptides with the first amino acid being neutral
    • C07K5/06017Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06026Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N5/00Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
    • C12N5/06Animal cells or tissues; Human cells or tissues
    • C12N5/0602Vertebrate cells
    • C12N5/0693Tumour cells; Cancer cells
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2500/00Specific components of cell culture medium
    • C12N2500/30Organic components
    • C12N2500/46Amines, e.g. putrescine
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Immunology (AREA)
  • Genetics & Genomics (AREA)
  • Biomedical Technology (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Oncology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Hematology (AREA)
  • Wood Science & Technology (AREA)
  • Radiology & Medical Imaging (AREA)
  • Zoology (AREA)
  • Pathology (AREA)
  • Biotechnology (AREA)
  • Diabetes (AREA)
  • Microbiology (AREA)
  • Cell Biology (AREA)
  • General Engineering & Computer Science (AREA)
  • Dermatology (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
CN201080031798.6A 2009-07-02 2010-06-25 Smac模拟物 Active CN102471275B (zh)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US22266809P 2009-07-02 2009-07-02
US61/222,668 2009-07-02
US12/819,221 2010-06-20
US12/819,221 US8283372B2 (en) 2009-07-02 2010-06-20 2-(1H-indol-3-ylmethyl)-pyrrolidine dimer as a SMAC mimetic
PCT/US2010/039976 WO2011002684A1 (fr) 2009-07-02 2010-06-25 Mimétique de smac

Publications (2)

Publication Number Publication Date
CN102471275A CN102471275A (zh) 2012-05-23
CN102471275B true CN102471275B (zh) 2014-05-28

Family

ID=43411387

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201080031798.6A Active CN102471275B (zh) 2009-07-02 2010-06-25 Smac模拟物

Country Status (27)

Country Link
US (10) US8283372B2 (fr)
EP (1) EP2448923B8 (fr)
JP (1) JP5674780B2 (fr)
KR (1) KR101755218B1 (fr)
CN (1) CN102471275B (fr)
AP (1) AP3619A (fr)
AR (1) AR077629A1 (fr)
AU (1) AU2010266525C1 (fr)
BR (1) BRPI1013958B1 (fr)
CA (1) CA2766162C (fr)
CL (1) CL2011003333A1 (fr)
CO (1) CO6480975A2 (fr)
DK (1) DK2448923T3 (fr)
EA (1) EA022061B1 (fr)
EC (1) ECSP11011557A (fr)
ES (1) ES2565337T3 (fr)
HK (2) HK1169410A1 (fr)
HU (1) HUE026982T2 (fr)
IL (1) IL217237A (fr)
MX (1) MX2011013819A (fr)
MY (1) MY153116A (fr)
NZ (1) NZ597051A (fr)
PE (1) PE20131173A1 (fr)
SG (1) SG177404A1 (fr)
TW (1) TWI485148B (fr)
WO (1) WO2011002684A1 (fr)
ZA (1) ZA201109342B (fr)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5230865B2 (ja) 2004-07-15 2013-07-10 テトラロジック ファーマシューティカルズ コーポレーション Iap結合性化合物
EP1851200B1 (fr) 2005-02-25 2014-01-15 Tetralogic Pharmaceuticals Corporation Inhibiteurs iap dimeriques
US20100317593A1 (en) * 2009-06-12 2010-12-16 Astrazeneca Ab 2,3-dihydro-1h-indene compounds
EP2448927B1 (fr) 2009-07-02 2014-03-12 Sanofi Nouveaux derives de (6-oxo-1,6-dihydro-pyrimidin-2-yl)-amide, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de phosphorylation d'akt
US8283372B2 (en) * 2009-07-02 2012-10-09 Tetralogic Pharmaceuticals Corp. 2-(1H-indol-3-ylmethyl)-pyrrolidine dimer as a SMAC mimetic
UY33236A (es) * 2010-02-25 2011-09-30 Novartis Ag Inhibidores dimericos de las iap
UY33794A (es) 2010-12-13 2012-07-31 Novartis Ag Inhibidores diméricos de las iap
JP2014528409A (ja) * 2011-09-30 2014-10-27 テトラロジック ファーマシューティカルズ コーポレーション 増殖性疾患(がん)の治療において使用するためのSMAC模倣体(ビリナパント(birinapant))
US20130196927A1 (en) * 2012-01-27 2013-08-01 Christopher BENETATOS Smac Mimetic Therapy
NZ704554A (en) * 2012-08-01 2015-12-24 Tetralogic Pharm Corp Combination therapy of a smac mimetic and gm-csf
AU2014301958B2 (en) 2013-06-25 2017-11-16 The Walter And Eliza Hall Institute Of Medical Research Method of treating intracellular infection
WO2015017520A1 (fr) * 2013-07-30 2015-02-05 Tetralogic Pharmaceuticals Corp. Procédé de traitement
WO2016079527A1 (fr) 2014-11-19 2016-05-26 Tetralogic Birinapant Uk Ltd Polythérapie
WO2016097773A1 (fr) 2014-12-19 2016-06-23 Children's Cancer Institute Antagonistes des iap thérapeutiques pour traiter des troubles prolifératifs
MX2018010202A (es) * 2016-02-24 2019-06-06 Childrens Hospital Of Eastern Ontario Res Institute Inc Terapia de combinacion con smc para el tratamiento de cancer.
RU2018141411A (ru) 2016-04-27 2020-05-27 Медшайн Дискавери Инк. Бензимидазол-связанное индольное соединение, выполняющее функцию нового двухвалентного антагониста iap
WO2019080928A1 (fr) * 2017-10-27 2019-05-02 南京明德新药研发股份有限公司 Forme cristalline d'un antagoniste d'iap et procédé de préparation correspondant
WO2019089991A1 (fr) * 2017-11-01 2019-05-09 The Regents Of The University Of California Nouveaux agents ciblant des protéines inhibitrices de l'apoptose
US10944377B2 (en) * 2017-12-31 2021-03-09 Skyworks Solutions, Inc. Broadband power splitter
WO2019154053A1 (fr) * 2018-02-09 2019-08-15 广东东阳光药业有限公司 Inhibiteur d'iap et leur utilisation en médecine
JPWO2020027225A1 (ja) 2018-07-31 2021-11-11 ファイメクス株式会社 複素環化合物
US10870663B2 (en) 2018-11-30 2020-12-22 Glaxosmithkline Intellectual Property Development Limited Compounds useful in HIV therapy
EP4006037A4 (fr) 2019-07-31 2023-12-13 Fimecs, Inc. Composé hétérocyclique
CN112521372B (zh) * 2019-09-18 2022-07-08 南京华威医药科技集团有限公司 一种细胞凋亡蛋白抑制剂及其制备方法和用途
CN112778398A (zh) * 2019-11-07 2021-05-11 杜心赟 肝靶向药、其药物组合物及其用途
EP4093394A1 (fr) 2020-01-20 2022-11-30 Astrazeneca AB Inhibiteurs de tyrosine kinase du récepteur du facteur de croissance épidermique pour le traitement du cancer
EP4262763A1 (fr) * 2020-12-17 2023-10-25 Council of Scientific & Industrial Research Mimétiques de smac pour le traitement du cancer, leur procédé de préparation et leur composition pharmaceutique
WO2023194547A1 (fr) 2022-04-08 2023-10-12 Medivir Ab Polymorphe h de birinapant
WO2023230432A1 (fr) 2022-05-23 2023-11-30 Inhibrx, Inc. Polythérapie à base d'agoniste de dr5 et d'antagoniste d'iap

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1926118A (zh) * 2004-03-01 2007-03-07 德克萨斯大学董事会 二聚的小分子细胞凋亡增强剂
WO2008014263A2 (fr) * 2006-07-24 2008-01-31 Tetralogic Pharmaceuticals Corporation Antagonistes des iap dimères
CN101128425A (zh) * 2005-02-25 2008-02-20 泰特拉洛吉克药业公司 Iap二聚体抑制剂

Family Cites Families (93)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3854480A (en) * 1969-04-01 1974-12-17 Alza Corp Drug-delivery system
US3832253A (en) * 1973-03-21 1974-08-27 Baxter Laboratories Inc Method of making an inflatable balloon catheter
DE2714880A1 (de) * 1977-04-02 1978-10-26 Hoechst Ag Cephemderivate und verfahren zu ihrer herstellung
EP0049898B2 (fr) 1980-10-15 1991-08-14 Takeda Chemical Industries, Ltd. Procédé d'essai immunochimique et trousse de réactifs
US4667014A (en) * 1983-03-07 1987-05-19 Syntex (U.S.A.) Inc. Nonapeptide and decapeptide analogs of LHRH, useful as LHRH antagonists
US4452775A (en) * 1982-12-03 1984-06-05 Syntex (U.S.A.) Inc. Cholesterol matrix delivery system for sustained release of macromolecules
CA1262014A (fr) 1983-01-07 1989-09-26 Mitsuaki Yoshida Peptides relies au virus de la leucemie humaine, anticorps de ces peptides et procede de production de ceux-ci
CA1200416A (fr) * 1983-05-13 1986-02-11 Societe Des Produits Nestle S.A. Procede de production de produit alimentaire
US5075109A (en) * 1986-10-24 1991-12-24 Southern Research Institute Method of potentiating an immune response
US4935493A (en) 1987-10-06 1990-06-19 E. I. Du Pont De Nemours And Company Protease inhibitors
US5208007A (en) * 1988-11-22 1993-05-04 Board Of Regents Of The University Of Oklahoma Isotopic tracer composition and method for making and using same
US5023077A (en) 1989-01-24 1991-06-11 Aphton Corporation Immunogenic compositions and methods for the treatment and prevention of gastric and duodenal ulcer disease
US5545719A (en) 1990-05-01 1996-08-13 Neuromedica, Inc. Nerve growth peptides
JPH04167172A (ja) * 1990-10-31 1992-06-15 Nec Corp ベクトルプロセッサ
DE4105480A1 (de) 1991-02-21 1992-08-27 Boehringer Mannheim Gmbh Verbesserte aktivierung von rekombinanten proteinen
US5831002A (en) 1992-05-20 1998-11-03 Basf Aktiengesellschaft Antitumor peptides
ES2130406T5 (es) * 1992-08-05 2003-12-16 Meito Sangyo Kk Material compuesto de pequeño diametro compuesto de carboxipolisacarido soluble en agua y oxido de hierro magnetico.
JP3401005B2 (ja) 1992-12-11 2003-04-28 ユニバーシティ オブ フロリダ 有害生物の防除のための材料および方法
US5468494A (en) 1993-11-12 1995-11-21 Aphton Corp. Immunogenic compositions against human gastrin 17
US5688506A (en) 1994-01-27 1997-11-18 Aphton Corp. Immunogens against gonadotropin releasing hormone
US5527775A (en) 1994-10-13 1996-06-18 Enzon, Inc. Reduction of mammalian neoplasms with phospholipase A2 activating substances
US6187557B1 (en) * 1995-08-08 2001-02-13 Tularik Inc. c-IAP1 and c-IAP2: inhibitors of apoptosis
US5786173A (en) * 1996-03-19 1998-07-28 Idun Pharmaceuticals, Inc. MCH4 and MCH5, apoptotic protease, nucleic acids encoding and methods of use
US6133437A (en) * 1997-02-13 2000-10-17 Apoptogen, Inc. Modulation of IAPs for the treatment of proliferative diseases
US5961955A (en) * 1997-06-03 1999-10-05 Coulter Pharmaceutical, Inc. Radioprotectant for peptides labeled with radioisotope
US5977311A (en) 1997-09-23 1999-11-02 Curagen Corporation 53BP2 complexes
US6110691A (en) * 2000-01-06 2000-08-29 Board Of Regents, The University Of Texas System Activators of caspases
US6608026B1 (en) * 2000-08-23 2003-08-19 Board Of Regents, The University Of Texas System Apoptotic compounds
EP1315811A2 (fr) 2000-08-24 2003-06-04 Thomas Jefferson University Peptide ou polypeptide capable de liaison avec l'inhibiteur de la proteine de l'apoptose
US6992063B2 (en) * 2000-09-29 2006-01-31 The Trustees Of Princeton University Compositions and method for regulating apoptosis
WO2004007529A2 (fr) 2002-07-15 2004-01-22 The Trustees Of Princeton University Composes qui se lient a iap
AU2001293189A1 (en) 2000-09-29 2002-04-08 Trustees Of Princeton University Compositions and methods for regulating apoptosis
WO2002030959A2 (fr) 2000-10-13 2002-04-18 Abbott Laboratories Peptides derives de smac (diablo) et procedes d'utilisation de ceux-ci
US20020160975A1 (en) * 2001-02-08 2002-10-31 Thomas Jefferson University Conserved XIAP-interaction motif in caspase-9 and Smac/DIABLO for mediating apoptosis
EP1421204A4 (fr) 2001-05-31 2004-12-15 Univ Princeton Peptides se liant a l'inhibiteur iap et dosages permettant d'identifier les composes qui se lient a l'inhibiteur iap
US7141589B2 (en) 2001-08-23 2006-11-28 The United States Of America As Represented By The Department Of Health And Human Services Methods of inhibiting formation of vascular channels and methods of inhibiting proliferation
EP1465649A4 (fr) * 2001-11-21 2007-07-11 Burnham Inst Methodes et compositions de derepression de caspase inhibee par un iap (inhibiteur de proteine d'apoptose)
US20060258581A1 (en) * 2001-11-21 2006-11-16 Reed John C Methods and composition for derepressions of IAP-inhibited caspase
AU2003249920A1 (en) 2002-07-02 2004-01-23 Novartis Ag Peptide inhibitors of smac protein binding to inhibitor of apoptosis proteins (iap)
US7149755B2 (en) 2002-07-29 2006-12-12 Hewlett-Packard Development Company, Lp. Presenting a collection of media objects
US20080199439A1 (en) 2003-02-12 2008-08-21 Mclendon George L IAP-binding cargo molecules and peptidomimetics for use in diagnostic and therapeutic methods
US7135575B2 (en) 2003-03-03 2006-11-14 Array Biopharma, Inc. P38 inhibitors and methods of use thereof
JP2007522116A (ja) * 2004-01-16 2007-08-09 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン コンホメーションが制約されたSmac模倣物およびその使用
JP2007523061A (ja) 2004-01-16 2007-08-16 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン Smacペプチドミメティクスおよびその使用法
BRPI0507482A (pt) 2004-02-05 2007-07-17 Novartis Ag combinação de (a) um inibidor de dna topoisomerase e (b) um inibidor de iap
US7345081B2 (en) * 2004-03-23 2008-03-18 Genentech, Inc. Azabicyclo-octane inhibitors of IAP
EP2253614B1 (fr) * 2004-04-07 2012-09-19 Novartis AG Inhibiteurs de IAP
US7244851B2 (en) * 2004-07-02 2007-07-17 Genentech, Inc. Inhibitors of IAP
US7674787B2 (en) 2004-07-09 2010-03-09 The Regents Of The University Of Michigan Conformationally constrained Smac mimetics and the uses thereof
BRPI0513310A (pt) 2004-07-12 2008-05-06 Idun Pharmaceuticals Inc análogos de tetrapeptìdeo
JP5230865B2 (ja) 2004-07-15 2013-07-10 テトラロジック ファーマシューティカルズ コーポレーション Iap結合性化合物
JP2008016458A (ja) 2004-08-18 2008-01-24 Teijin Ltd 電磁波吸収シート材料
EA019420B1 (ru) 2004-12-20 2014-03-31 Дженентех, Инк. Пирролидиновые ингибиторы иап (ингибиторов апоптоза)
US20060228352A1 (en) * 2005-02-24 2006-10-12 Schoenberger Stephen P TRAIL and methods of modulating T cell activity and adaptive immune responses using TRAIL
EP1851200B1 (fr) * 2005-02-25 2014-01-15 Tetralogic Pharmaceuticals Corporation Inhibiteurs iap dimeriques
US20070003535A1 (en) * 2005-03-17 2007-01-04 Reed John C Methods and compositions for derepression of IAP-inhibited caspase
US7763604B2 (en) 2005-05-16 2010-07-27 Thallion Pharma Ceuticals, Inc. Methods for administration of a farnesyl dibenzodiazepinone
EP1883627B1 (fr) * 2005-05-18 2018-04-18 Pharmascience Inc. Composes liants de domaine bir
AU2006254538A1 (en) 2005-05-25 2006-12-07 2Curex Aps Compounds modifying apoptosis
MX2007015419A (es) 2005-06-08 2008-02-21 Novartis Ag Compuestos organicos.
JP2009509128A (ja) * 2005-08-09 2009-03-05 テトラロジック ファーマシューティカルズ コーポレーション 増殖性疾患の治療
US20070203749A1 (en) 2005-08-09 2007-08-30 Sri Chunduru Business methods for compounds for treatment of proliferative disorders
AU2006308453B9 (en) * 2005-10-25 2011-12-01 Pharmascience Inc. IAP BIR domain binding compounds
KR20080080203A (ko) 2005-12-19 2008-09-02 제넨테크, 인크. Iap의 억제제
JP5227805B2 (ja) * 2005-12-20 2013-07-03 ノバルティス アーゲー Iap阻害剤とタキサン7の組合せ剤
WO2007101347A1 (fr) 2006-03-07 2007-09-13 Aegera Therapeutics Inc. Composés de liaison au domaine bir
TWI504597B (zh) * 2006-03-16 2015-10-21 Pharmascience Inc 結合於細胞凋亡抑制蛋白(iap)之桿狀病毒iap重複序列(bir)區域之化合物
MX2008012053A (es) * 2006-03-21 2008-12-17 Joyant Pharmaceuticals Inc Promotores de apoptosis de molecula pequeña.
CN101484151B (zh) 2006-05-05 2012-11-21 密执安州立大学董事会 二价smac模拟物及其应用
US8202902B2 (en) * 2006-05-05 2012-06-19 The Regents Of The University Of Michigan Bivalent SMAC mimetics and the uses thereof
AU2007250443B2 (en) * 2006-05-16 2013-06-13 Pharmascience Inc. IAP BIR domain binding compounds
WO2008014240A2 (fr) 2006-07-24 2008-01-31 Tetralogic Pharmaceuticals Corporation Inhibiteurs des iap dimères
WO2008014238A2 (fr) 2006-07-24 2008-01-31 Tetralogic Pharmaceuticals Corporation Inhibiteurs des iap dimères
WO2008014252A2 (fr) 2006-07-24 2008-01-31 Tetralogic Pharmaceuticals Corporation Inhibiteurs des iap
US20100144650A1 (en) 2006-07-24 2010-06-10 Tetralogic Pharmaceuticals Corporation Dimeric iap inhibitors
WO2008014236A1 (fr) 2006-07-24 2008-01-31 Tetralogic Pharmaceuticals Corporation Inhibiteurs d'iap dimériques
PE20110220A1 (es) 2006-08-02 2011-04-11 Novartis Ag DERIVADOS DE 2-OXO-ETIL-AMINO-PROPIONAMIDA-PIRROLIDIN-2-IL-SUSTITUIDOS COMO INHIBIDORES DEL ENLACE DE LA PROTEINA Smac AL INHIBIDOR DE LA PROTEINA DE APOPTOSIS
JP2010507096A (ja) 2006-10-19 2010-03-04 ノバルティス アーゲー 有機化合物
JP2010513561A (ja) * 2006-12-19 2010-04-30 ジェネンテック, インコーポレイテッド Iapのイミダゾピリジンインヒビター
US8642554B2 (en) * 2007-04-12 2014-02-04 Joyant Pharmaceuticals, Inc. Smac mimetic dimers and trimers useful as anti-cancer agents
CA2683392A1 (fr) 2007-04-30 2008-11-06 Genentech, Inc. Inhibiteurs de iap
JP2010528587A (ja) 2007-05-07 2010-08-26 テトラロジック ファーマシューティカルズ コーポレーション アポトーシス阻害タンパク質のアンタゴニストに対する感受性のバイオマーカーとしてTNFα遺伝子の発現を用いる方法
AU2009206588A1 (en) 2008-01-24 2009-07-30 Tetralogic Pharmaceuticals Corporation IAP inhibitors
WO2010033531A1 (fr) 2008-09-17 2010-03-25 Tetralogic Pharmaceuticals Corp. Inhibiteurs d’iap
EP2382465A1 (fr) 2009-01-29 2011-11-02 Otto-von-Guericke-Universität Magdeburg Procédé de détermination de sensibilité de cellules humaines ou animales non humaines à un antagoniste de iap
NZ596669A (en) 2009-05-28 2013-11-29 Tetralogic Pharm Corp Iap inhibitors
EP2434890A4 (fr) 2009-05-28 2013-01-02 Tetralogic Pharm Corp Inhibiteurs de protéines d'apoptose
US8283372B2 (en) 2009-07-02 2012-10-09 Tetralogic Pharmaceuticals Corp. 2-(1H-indol-3-ylmethyl)-pyrrolidine dimer as a SMAC mimetic
JP2014528409A (ja) 2011-09-30 2014-10-27 テトラロジック ファーマシューティカルズ コーポレーション 増殖性疾患(がん)の治療において使用するためのSMAC模倣体(ビリナパント(birinapant))
US20130196927A1 (en) 2012-01-27 2013-08-01 Christopher BENETATOS Smac Mimetic Therapy
NZ704554A (en) 2012-08-01 2015-12-24 Tetralogic Pharm Corp Combination therapy of a smac mimetic and gm-csf
WO2014121178A1 (fr) 2013-02-04 2014-08-07 Tetralogic Pharmaceuticals Corp. Procédé de traitement par mimétique de smac
US20140303090A1 (en) 2013-04-08 2014-10-09 Tetralogic Pharmaceuticals Corporation Smac Mimetic Therapy

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1926118A (zh) * 2004-03-01 2007-03-07 德克萨斯大学董事会 二聚的小分子细胞凋亡增强剂
CN101128425A (zh) * 2005-02-25 2008-02-20 泰特拉洛吉克药业公司 Iap二聚体抑制剂
WO2008014263A2 (fr) * 2006-07-24 2008-01-31 Tetralogic Pharmaceuticals Corporation Antagonistes des iap dimères

Also Published As

Publication number Publication date
EP2448923A4 (fr) 2013-05-01
JP2012532129A (ja) 2012-12-13
US10034912B2 (en) 2018-07-31
HK1171022A1 (en) 2013-03-15
JP5674780B2 (ja) 2015-02-25
US20110003877A1 (en) 2011-01-06
AU2010266525B2 (en) 2015-05-21
US8603816B2 (en) 2013-12-10
PE20131173A1 (es) 2013-10-03
CO6480975A2 (es) 2012-07-16
US20170182116A1 (en) 2017-06-29
US11351221B2 (en) 2022-06-07
US10596220B2 (en) 2020-03-24
ES2565337T3 (es) 2016-04-04
IL217237A0 (en) 2012-02-29
US8283372B2 (en) 2012-10-09
US20230149500A1 (en) 2023-05-18
WO2011002684A1 (fr) 2011-01-06
BRPI1013958B1 (pt) 2022-04-05
EP2448923A1 (fr) 2012-05-09
TW201113276A (en) 2011-04-16
AP3619A (en) 2016-02-29
AR077629A1 (es) 2011-09-14
AP2012006066A0 (en) 2012-02-29
KR101755218B1 (ko) 2017-07-07
AU2010266525C1 (en) 2015-10-01
ECSP11011557A (es) 2012-06-29
CL2011003333A1 (es) 2012-07-20
IL217237A (en) 2014-09-30
TWI485148B (zh) 2015-05-21
DK2448923T3 (en) 2016-02-29
SG177404A1 (en) 2012-02-28
MY153116A (en) 2014-12-31
KR20120047905A (ko) 2012-05-14
NZ597051A (en) 2013-10-25
EP2448923B1 (fr) 2015-11-25
AU2010266525A1 (en) 2012-01-19
CA2766162C (fr) 2018-07-24
US20140073579A1 (en) 2014-03-13
EA201171494A1 (ru) 2012-06-29
CN102471275A (zh) 2012-05-23
HUE026982T2 (en) 2016-08-29
CA2766162A1 (fr) 2011-01-06
MX2011013819A (es) 2012-06-08
US20130012564A1 (en) 2013-01-10
EA022061B1 (ru) 2015-10-30
BRPI1013958A2 (pt) 2019-09-03
ZA201109342B (en) 2014-05-28
US20120115922A1 (en) 2012-05-10
US20180303897A1 (en) 2018-10-25
HK1169410A1 (zh) 2013-01-25
US20150158908A1 (en) 2015-06-11
US8986993B2 (en) 2015-03-24
EP2448923B8 (fr) 2016-01-27
US20190255139A1 (en) 2019-08-22
US10314881B2 (en) 2019-06-11
US20200282002A1 (en) 2020-09-10
US11951147B2 (en) 2024-04-09

Similar Documents

Publication Publication Date Title
CN102471275B (zh) Smac模拟物
EP3601258B1 (fr) Dérivés d'isoquinoléine substitués utilisés en tant qu'immunomutateurs
JP5452811B2 (ja) 有糸分裂進行を阻害するための化合物
KR101915452B1 (ko) 백금 화합물, 조성물 및 이의 용도
CN109641910A (zh) 吡咯并苯二氮*及其缀合物
TW200808746A (en) Triazole compounds that modulate HSP90 activity
CA2850330A1 (fr) Mimetique de smac (birinapant) a utiliser dans le traitement de maladies de proliferation (cancer)
WO2018191587A1 (fr) Inhibiteurs de kinases tam
EP4061818B1 (fr) Peptides macrocycliques en tant qu'inhibiteurs de pd-l1 et immunomodulateurs pour le traitement du cancer et de maladies infectieuses
EP3922251A1 (fr) Adjuvant d'immunothéraphie anticancéreuse
CN104829596A (zh) 吡咯取代吲哚酮类衍生物、其制备方法、包含该衍生物的组合物、及其用途
CN101454309A (zh) 焦谷氨酸衍生物的合成和用途
EP3851108B1 (fr) Médicament à base de borate et utilisation associée
CN102906086B (zh) 喹唑啉化合物
WO2020232401A1 (fr) Polythérapies avec des inhibiteurs à petites molécules ire1
EP3125901B1 (fr) Dérivés de céphalosporines pour traiter le cancer
CN103965175A (zh) 4-(取代苯氨基)喹唑啉类化合物、其制备方法及应用
CN117545479A (zh) Pi3k抑制剂、纳米制剂及其用途
KR101480481B1 (ko) 퀴나졸린 화합물
CN109312157A (zh) 治疗癌症的lls化合物
CN111018739A (zh) 一种氨甲环酸衍生物及其制备方法和在制备治疗口腔癌药物中的用途

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
REG Reference to a national code

Ref country code: HK

Ref legal event code: DE

Ref document number: 1171022

Country of ref document: HK

C14 Grant of patent or utility model
GR01 Patent grant
REG Reference to a national code

Ref country code: HK

Ref legal event code: GR

Ref document number: 1171022

Country of ref document: HK

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20170809

Address after: West Midlands

Patentee after: Tate jeek bilina Lalo pant UK Ltd

Address before: American Pennsylvania

Patentee before: Tetralogic Pharmaceuticals

CP02 Change in the address of a patent holder
CP02 Change in the address of a patent holder

Address after: England

Patentee after: Tate jeek bilina Lalo pant UK Ltd

Address before: West Midlands

Patentee before: Tate jeek bilina Lalo pant UK Ltd

TR01 Transfer of patent right

Effective date of registration: 20190920

Address after: Hu Dinge, Sweden

Patentee after: Medville Co., Ltd.

Address before: England

Patentee before: Tate jeek bilina Lalo pant UK Ltd

TR01 Transfer of patent right